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NCT ID: NCT05067166 Available - Clinical trials for Hemorrhagic Fever, Ebola

Open-Label Expanded Access for Ebola-Infected Patients to Receive Human mAb Ansuvimab as Therapeutic or for HR PEP

Start date: n/a
Phase:
Study type: Expanded Access

The human monoclonal antibody (mAb), ansuvimab (mAb114), will be provided to Ebola-infected patients as either a treatment or as PEP under expanded access. Ansuvimab is administered at 50 mg/kg as a single intravenous (IV) infusion

NCT ID: NCT05095116 Available - Clinical trials for Eosinophilic Esophagitis

Expanded Access Protocol for Patients With Eosinophilic Esophagitis

Start date: n/a
Phase:
Study type: Expanded Access

This expanded access program is an open-label, single-arm design where consenting patients may participate up until APT-1011 is commercially available in the relevant regions or the protocol is terminated by the Sponsor.

NCT ID: NCT05100134 Available - Clinical trials for Non-small Cell Lung Cancer (NSCLC)

Managed Access Programs for LDK378, Ceritinib

Start date: n/a
Phase:
Study type: Expanded Access

The purpose of this registration is to list Managed Access Programs (MAPs) related to LDK378, Ceritinib.

NCT ID: NCT05119257 Available - Cancer Clinical Trials

(Bispecific) Antibodies in Cancer Patients

InHeAb01
Start date: n/a
Phase:
Study type: Expanded Access

The aim of this project is to provide (bispecific) antibodies to individual patients with advanced solid and hematological malignancies without any available approved treatment options.

NCT ID: NCT05134922 Available - Clinical trials for Breast Neoplasm Malignant Female

Expanded Access Protocol for Subjects Previously Treated With Gedatolisib in B2151009

Start date: n/a
Phase:
Study type: Expanded Access

Continued access to treatment for subjects who continue benefit from therapy with gedatolisib in combination with palbociclib, and fulvestrant or letrozole.

NCT ID: NCT05151679 Available - Clinical trials for Iron Deficiency Anemia of Pregnancy

Chelated Oral Iron Versus Intravenous Iron Sucrose for Treatment of Iron Deficiency Anemia Late in Pregnancy

Start date: n/a
Phase:
Study type: Expanded Access

compare the efficacy and safety of intravenous iron sucrose versus chelated oral iron in the treatment of iron deficiency anemia late in pregnancy.

NCT ID: NCT05164250 Available - Multiple Myeloma Clinical Trials

Compassionate Use (CU) of REGN5458 for Patients With Relapsed or Refractory Multiple Myeloma (MM)

Start date: n/a
Phase:
Study type: Expanded Access

Provide Compassionate Use' of REGN5458 for Patients with Relapsed or Refractory Multiple Myeloma

NCT ID: NCT05170724 Available - Clinical trials for Chronic Spontaneous Urticaria

Global Managed Access Program Cohort for Remibrutinib in Adult Patients With Chronic Spontaneous Urticaria

Start date: n/a
Phase:
Study type: Expanded Access

The purpose of this Managed Access Program (MAP) Cohort Treatment Plan is to provide access to remibrutinib for adult patients with chronic spontaneous urticaria (CSU)

NCT ID: NCT05172700 Available - Clinical trials for Waldenstrom Macroglobulinemia

Expanded Access Program for Pirtobrutinib for Participants With B-Cell Cancer

Start date: n/a
Phase:
Study type: Expanded Access

This is an expanded access program for eligible participants with a previously treated B-cell cancer who are ineligible for an ongoing pirtobrutinib clinical trial. The treating physician/investigator contacts Lilly when, based on their medical opinion, a patient meets the criteria for inclusion in the expanded access program.

NCT ID: NCT05215288 Available - Clinical trials for Solid Organ Transplant Rejection

Expanded Access for Use of ExoFlo in Abdominal Solid Organ Transplant Patients

Start date: n/a
Phase:
Study type: Expanded Access

This Expanded Access Protocol will provide access to the IMP ExoFlo for patients who have severe or life-threatening abdominal solid organ transplant rejection or who are evaluated and determined to be at high risk of progression to severe or life-threatening condition related to rejection of an abdominal solid organ transplant, at risk of worsening allograft function, or at risk of complications from current immunosuppressive therapeutic regimens.